NP-MRD: Showing NP-Card for 1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione (NP0290279)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 20:53:14 UTC

Updated at

2022-09-09 20:53:14 UTC

NP-MRD ID

NP0290279

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione

Description

1,4,6B,7,10-pentahydroxy-1,2,6b,7,8,12b-hexahydroperylene-3,9-dione belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. 1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione is found in Alternaria tenuissima. Based on a literature review very few articles have been published on 1,4,6b,7,10-pentahydroxy-1,2,6b,7,8,12b-hexahydroperylene-3,9-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092222532D          

 27 31  0  0  0  0            999 V2000
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
  6 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END

     RDKit          3D

 43 47  0  0  0  0  0  0  0  0999 V2000
   -4.7873   -0.3298   -0.5148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7234    0.0168    0.0181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5541    1.3678    0.6085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2237    1.8824    0.0646 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2318    1.9750   -1.3057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1305    0.9942    0.6091 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1868    1.4096    0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3876    2.6364   -0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6022    3.0480   -0.9912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259    2.2062   -0.9149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8764    2.7210   -1.4246 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5315    0.9650   -0.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2863    0.5485    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1223   -0.7855    0.7603 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1846   -0.6514    2.1644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2482   -1.2825    0.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570   -2.6257    0.2202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7140   -3.1352   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7713   -2.2490   -0.1396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0415   -2.7263   -0.4330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6014   -0.9006    0.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3229   -0.4322    0.3729 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1625   -1.7288    0.2840 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9989   -2.0034   -1.0531 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5483   -1.1718    0.4972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7066    0.1087   -0.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8210    0.3609   -0.7270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3632    2.0623    0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4386    1.2635    1.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    2.8819    0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6926    2.8165   -1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1678    1.1460    1.7255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4899    3.3038   -0.5702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6755    4.0411   -1.4344 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7743    2.3570   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2707   -0.5934    2.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3314   -3.3496    0.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8716   -4.1971   -0.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2616   -3.6821   -0.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1608   -2.7048    0.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7549   -2.6149   -1.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8247   -1.0475    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2540   -1.9009    0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 21  1  0
 21 22  2  0
 22  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  1
 14 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
  6  4  1  0
 13  7  1  0
 19 21  1  0
 16 22  1  0
 26 12  1  0
  5 31  1  0
  4 30  1  1
  3 28  1  0
  3 29  1  0
  6 32  1  1
  8 33  1  0
  9 34  1  0
 11 35  1  0
 15 36  1  0
 23 40  1  1
 24 41  1  0
 25 42  1  0
 25 43  1  0
 17 37  1  0
 18 38  1  0
 20 39  1  0
M  END


  Mrv1652309092222532D          

 27 31  0  0  0  0            999 V2000
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
  6 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0290279

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1CC(=O)C2=C3C1C1=CC=C(O)C4=C1C(O)(C(O)CC4=O)C3=CC=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O7/c21-9-4-2-8-16-15(11(23)5-12(24)17(9)16)7-1-3-10(22)18-13(25)6-14(26)20(8,27)19(7)18/h1-4,11,14-15,21-23,26-27H,5-6H2

> <INCHI_KEY>
VJWXYPUJILLMFB-UHFFFAOYSA-N

> <FORMULA>
C20H16O7

> <MOLECULAR_WEIGHT>
368.341

> <EXACT_MASS>
368.089602855

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
35.816261043307925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,4,6b,7,10-pentahydroxy-1,2,3,6b,7,8,9,12b-octahydroperylene-3,9-dione

> <JCHEM_LOGP>
0.936307805

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.84622279764111

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.242894073324747

> <JCHEM_PKA_STRONGEST_BASIC>
-3.036393250703047

> <JCHEM_POLAR_SURFACE_AREA>
135.29000000000002

> <JCHEM_REFRACTIVITY>
94.00749999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1H-perylene-3,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.002   4.620   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335  -1.540   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   22                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   26                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15   16   23                                             
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    2   22                                                  
CONECT   22   21   16    6                                                  
CONECT   23   14   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   12   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₇

Average Mass

368.3410 Da

Monoisotopic Mass

368.08960 Da

IUPAC Name

1,4,6b,7,10-pentahydroxy-1,2,3,6b,7,8,9,12b-octahydroperylene-3,9-dione

Traditional Name

1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1H-perylene-3,9-dione

CAS Registry Number

Not Available

SMILES

OC1CC(=O)C2=C3C1C1=CC=C(O)C4=C1C(O)(C(O)CC4=O)C3=CC=C2O

InChI Identifier

InChI=1S/C20H16O7/c21-9-4-2-8-16-15(11(23)5-12(24)17(9)16)7-1-3-10(22)18-13(25)6-14(26)20(8,27)19(7)18/h1-4,11,14-15,21-23,26-27H,5-6H2

InChI Key

VJWXYPUJILLMFB-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Alternaria tenuissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Anthracene
Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Tertiary alcohol
Secondary alcohol
Ketone
Polyol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.94	ChemAxon
pKa (Strongest Acidic)	8.24	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	135.29 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.01 m³·mol⁻¹	ChemAxon
Polarizability	35.82 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162787889

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione (NP0290279)

MOL for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

3D MOL for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

3D SDF for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

3D-SDF for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

PDB for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

3D PDB for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

SMILES for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

INCHI for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

Structure for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)

3D Structure for NP0290279 (1,4,6b,7,10-pentahydroxy-2,7,8,12b-tetrahydro-1h-perylene-3,9-dione)